Novel ALDH3A2 heterozygous mutations in a Japanese family with Sjögren-Larsson syndrome

J Invest Dermatol. 2006 Nov;126(11):2545-7. doi: 10.1038/sj.jid.5700453. Epub 2006 Jun 22.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aldehyde Oxidoreductases / genetics*
  • Amino Acid Sequence
  • Asian People
  • Child, Preschool
  • DNA Mutational Analysis
  • Female
  • Heterozygote*
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Pedigree
  • Sjogren-Larsson Syndrome / diagnosis
  • Sjogren-Larsson Syndrome / genetics*
  • Sjogren-Larsson Syndrome / pathology

Substances

  • Aldehyde Oxidoreductases
  • long-chain-aldehyde dehydrogenase